Digestive and absorptive functions of the small intestines Flashcards

1
Q

What are the nutritionally important carbohydrates?

A

Starch (amylose & amylopectin), disaccharides (sucrose, lactose), monosaccharides (glucose, galactose, fructose), and dietary fibers.

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2
Q

How are glucose and galactose absorbed?

A

Via secondary active transport using SGLT-1 (sodium-glucose cotransporter).

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2
Q

Salivary amylase and pancreatic amylase.

A

Maltose (2 glucose units), maltotriose (3 glucose units), and α-limit dextrins (5-6 glucose units).

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2
Q

What enzymes are involved in luminal digestion of carbohydrates?

A

Salivary amylase and pancreatic amylase.

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2
Q

What is the role of pepsin in protein digestion?

A

Pepsin digests dietary proteins at neutral amino acids in the stomach (prefers low pH).

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3
Q

How is fructose absorbed?

A

By facilitated diffusion via GLUT5 transporter.

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4
Q

What activates trypsinogen to trypsin?

A

Enterokinase in the duodenum.

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5
Q

How are di- and tripeptides absorbed?

A

Via PEPT1 transporter coupled with H⁺ ions.

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6
Q

What are the four systems for amino acid absorption?

A

Neutral, basic, proline/glycine, and dicarboxylic (glutamic/aspartic acids).

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6
Q

What is the role of bile salts in lipid digestion?

A

Emulsify fats and form micelles for absorption.

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6
Q

How are monoglycerides and FFAs absorbed?

A

Passive diffusion from micelles into enterocytes.

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7
Q

What happens to long-chain FFAs (>12 carbons) after absorption?

A

Re-esterified into triglycerides and packaged into chylomicrons for lymphatic transport.

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8
Q

What is the role of colipase?

A

What is the role of colipase?

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9
Q

How is vitamin B₁₂ absorbed?

A

Bound to intrinsic factor (IF) in the ileum via IF-cobalamin receptors.

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10
Q

What enhances iron (Fe²⁺) absorption?

A

Gastric acid (reduces Fe³⁺ to Fe²⁺) and ascorbic acid (vitamin C).

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11
Q

How is calcium absorption regulated?

A

Active transport stimulated by vitamin D₃; inhibited by phosphates/oxalates.

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11
Q

What causes lactose intolerance?

A

Decline in brush border lactase enzyme, leading to undigested lactose fermented by colonic bacteria (bloating, diarrhea).

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12
Q

What is celiac disease?

A

Autoimmune reaction to gluten (α-gliadin), damaging intestinal villi and causing malabsorption.

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13
Q

What is glucose-galactose malabsorption?

A

Mutation in SGLT-1 transporter, causing severe diarrhea; treated with fructose-substituted diets.

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13
Q

How does cholera toxin cause diarrhea?

A

Activates adenylate cyclase → ↑cAMP → ↑Cl⁻ secretion and ↓Na⁺ absorption in the intestine.

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14
Q

Where is most water reabsorbed in the GI tract?

A

Jejunum (5500 ml/day), ileum (2000 ml/day), and colon (1300 ml/day).

14
Q

How does aldosterone affect Na⁺ absorption?

A

Enhances Na⁺ reabsorption in the ileum and colon by upregulating Na⁺/K⁺ ATPase.

15
Q

What is the role of CFTR in secretory diarrhea?

A

CFTR channel secretes Cl⁻ into the lumen, followed by Na⁺ and water (e.g., in cholera).

15
Q

Which enzyme digests amylose and amylopectin, and what are its products?

A

Pancreatic amylase; produces maltose, maltotriose, and α-limit dextrins.

15
What brush border enzymes digest disaccharides?
Sucrase (sucrose → glucose + fructose), lactase (lactose → glucose + galactose), maltase (maltose → 2 glucose).
15
What is the role of enterokinase?
Activates trypsinogen → trypsin in the duodenum, initiating protein digestion.
16
Which pancreatic enzyme hydrolyzes triglycerides at positions 1 and 3?
Pancreatic lipase (requires colipase to function in the presence of bile salts).
16
What enzyme breaks down cholesterol esters?
Cholesterol esterase (also digests triglycerides and vitamin esters).
17
How are small peptides absorbed?
Via PEPT1 (H⁺-coupled cotransporter) into enterocytes.
17
What transporter absorbs vitamin C, and how is it regulated?
SVCT1/SVCT2 (Na⁺-dependent); downregulated by high vitamin C intake.
18
How does fructose absorption differ from glucose/galactose?
Fructose uses GLUT5 (facilitated diffusion), while glucose/galactose use SGLT-1 (active transport).
19
What happens if SGLT-1 is defective?
Glucose-galactose malabsorption → osmotic diarrhea, managed with fructose diets.
20
How are nucleic acids absorbed?
Nucleases → nucleotides → nucleosides + phosphate → sugars + bases (absorbed actively).
21
What is the composition of a micelle?
Bile salts, monoglycerides, FFAs, cholesterol, and fat-soluble vitamins.
21
Why are micelles critical for fat absorption?
Solubilize hydrophobic lipids for diffusion across the unstirred water layer.
21
What happens to absorbed long-chain FFAs?
Re-esterified into triglycerides → packaged into chylomicrons → lymphatics.
22
Why do pancreatic insufficiency patients have steatorrhea?
Lack of lipase and colipase → impaired micelle formation → fat malabsorption.
22
What causes lactose intolerance symptoms?
Undigested lactose → bacterial fermentation → gas (H₂/CO₂), osmotic diarrhea.
22
How is celiac disease managed?
Strict gluten-free diet (avoid wheat/barley/rye) to prevent villous atrophy.
22
What is Hartnup disease?
Defect in neutral AA transport (e.g., tryptophan) → pellagra-like symptoms; treated with nicotinamide.
22
Why does gastrectomy cause iron deficiency anemia?
Loss of gastric acid → impaired reduction of Fe³⁺ to absorbable Fe²⁺.
22
How does cholera toxin disrupt fluid balance?
↑cAMP → CFTR activation → Cl⁻ secretion → Na⁺/water follow → secretory diarrhea.
23
What is the pathophysiology of cystic fibrosis-related malabsorption?
Thick mucus blocks pancreatic enzyme secretion → fat/protein maldigestion.
24
Why are oral rehydration solutions (ORS) effective?
Glucose enhances Na⁺ absorption via SGLT-1 → osmotic water reabsorption.
25
Where is most NaCl absorbed?
Jejunum (nutrient-coupled) and colon (aldosterone-dependent electrogenic absorption).
25
Why are breast milk lipases important for neonates?
Compensate for immature pancreatic function (e.g., bile salt-stimulated lipase).
25
What inhibits calcium absorption?
Phosphates, oxalates (form insoluble salts); enhanced by lactose/vitamin D₃.
26
How is vitamin B₁₂ transported in blood?
Bound to transcobalamin II (defects cause megaloblastic anemia).
26
How does the colon secrete bicarbonate?
Cl⁻/HCO₃⁻ exchanger (pendrin) at the apical membrane; driven by basolateral Na⁺/K⁺ ATPase.
27
What is the role of NHE3 in the intestine?
Apical Na⁺/H⁺ exchanger (electroneutral NaCl absorption in small intestine/colon).